Cleared Traditional

K800067 - VITA LAMP, MODEL 0350

K800067 is an FDA 510(k) clearance for VITA LAMP, manufactured by Tensor Industries, Inc.. The device is a Class 1 General Hospital device with product code KZF cleared through the Traditional 510(k) pathway after a 118-day FDA review.

K800067 · Tensor Industries, Inc. · General Hospital
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May 1980
Decision
118d
Days
Class 1
Risk

K800067 is an FDA 510(k) clearance for the VITA LAMP, MODEL 0350. Classified as Device, Medical Examination, Ac Powered (product code KZF), Class I - General Controls.

Submitted by Tensor Industries, Inc. (Mchenry, US). The FDA issued a Cleared decision on May 8, 1980 after a review of 118 days - within the typical 510(k) review window.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6320 - the FDA general hospital device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General Hospital review framework, consistent with the majority of Class II 510(k) submissions.

View all Tensor Industries, Inc. devices

FDA 510(k) Submission Details - K800067

510(k) Number K800067 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 11, 1980
Decision Date May 08, 1980
Days to Decision 118 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
11d faster than avg
Panel avg: 129d · This submission: 118d
Pathway characteristics
Predicate-based equivalence.

KZF Device Classification - Class 1, General Controls

Product Code KZF Device, Medical Examination, Ac Powered
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.6320
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - KZF Device, Medical Examination, Ac Powered

All 15
Devices cleared under the same product code (KZF) and FDA review panel - the closest regulatory comparables to K800067.
OLYMPIC LIGHT-WARM
K896611 · Olympic Medical Corp. · Feb 1990
TINY HALOGEN EXAM LIGHT
K896962 · Jedmed Instrument Co. · Dec 1989
WELCH ALLYN #48100 TASK LITE W/ACCESSORIES AS LIST
K852949 · Welch Allyn, Inc. · Sep 1985
ABCO EXAMINATION LAMP (GOOSENECK TYPE)
K800230 · Abco Dealers, Inc. · Feb 1980
HALOGEN EXAM. LITE #48400
K780628 · Welch Allyn, Inc. · Jun 1978